成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart Sign in  
Chemical Structure| 93-10-7 Chemical Structure| 93-10-7
Chemical Structure| 93-10-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

{[proInfo.proName]}

CAS No.: 93-10-7

,{[proInfo.pro_purity]}

Quinoline-2-carboxylic Acid is an endogenous metabolite used to explore its role in biochemistry and drug research.

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Quinoline-2-carboxylic acid

CAS No. :93-10-7
Formula : C10H7NO2
M.W : 173.17
SMILES Code : C1=CC=CC2=CC=C(N=C12)C(O)=O
MDL No. :MFCD00006752
InChI Key :LOAUVZALPPNFOQ-UHFFFAOYSA-N
Pubchem ID :7124

Safety of Quinoline-2-carboxylic acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Quinoline-2-carboxylic acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 93-10-7 ]

[ 93-10-7 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 93-10-7 ]
  • [ 2899-28-7 ]
  • [ 82827-38-1 ]
  • 2
  • [ 93-10-7 ]
  • [ 4089-07-0 ]
  • [ 82827-37-0 ]
  • 4
  • [ 93-10-7 ]
  • [ 3171-46-8 ]
  • [ 1339147-56-6 ]
  • 5
  • [ 93-10-7 ]
  • [ 600-05-5 ]
  • C13H11BrNO4(1+)*Br(1-) [ No CAS ]
  • 6
  • [ 93-10-7 ]
  • [ 40963-14-2 ]
  • N-(1-carbamoyl-1,2-dimethylpropyl)-2-quinolinecarboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; water; EXAMPLE 55 Preparation of N-(1-carbamoyl-1,2-dimethylpropyl)quinaldamide STR203 To a solution of quinaldic acid (20 g, 0.116 mol) in tetrahydrofuran (500 ml) cooled to -9 C. is added methyl chloroformate (8.92 ml, 0.116 mol) followed by triethylamine (18.4 ml, 0.139 mol). After 20 minutes <strong>[40963-14-2]2-amino-2,3-dimethylbutyramide</strong> (15.1 g, 0.116 mol) is added and the mixture stirred overnight at room temperature. Water is added and the solution is reduced to 200 ml of a rotorvap. A white solid separates and is filtered off, water washed and dried. Recrystallization from absolute ethanol gives the product mp 179-180 C., 26.86 g (87%). Anal. calcd. for C16 H19 N3 O2: C, 67.34; H, 6.73; N, 14.72. Found: C, 67.14; H, 6.17; N, 14.72.
  • 7
  • [ 93-10-7 ]
  • [ 36887-98-6 ]
  • C19H17N3O [ No CAS ]
 

Historical Records

Technical Information

Categories